Evidence map›Paper›PMID 26964669›Full record

ArticleNature communications2016

IL-15-dependent balance between Foxp3 and RORγt expression impacts inflammatory bowel disease.

Milena J Tosiek, Laurence Fiette, Sary El Daker, Gérard Eberl, Antonio A Freitas

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 75 citations in OpenAlex.

  1. T-betThe FEBS journal · 2026
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  11. Selected Cytokines and Metalloproteinases in Inflammatory Bowel Disease.International journal of molecular sciences · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Milena J TosiekUnité de Biologie des Populations Lymphocytaires, Department of Immunology, Institut Pasteur, 25, rue du Docteur Roux, 75015 Paris, France.
Laurence FietteUnité d'Histopathologie Humaine et Modèles Animaux, Department of Infection and Epidemiology, Institut Pasteur, Hôpital Ste Anne, 75015 Paris, France.
Sary El DakerUnité de Biologie des Populations Lymphocytaires, Department of Immunology, Institut Pasteur, 25, rue du Docteur Roux, 75015 Paris, France.
Gérard EberlCNRS, URA1961, 75015 Paris, France.
Antonio A FreitasUnité de Biologie des Populations Lymphocytaires, Department of Immunology, Institut Pasteur, 25, rue du Docteur Roux, 75015 Paris, France.
Centre National de la Recherche Scientifique · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability of CD4+ T cells to change their phenotype and to specialize into different functional subsets may enhance the risk of autoimmune diseases. Here we investigate how a pleiotropic cytokine interleukin (IL)-15 may modify the functional commitment of CD4+ T cells expressing the lineage-associated transcription factors: forkhead box P3 (Foxp3; Treg) and RORγt (Th17) in the context of inflammatory bowel disease (IBD). We demonstrate in mice that impaired delivery of IL-15 to CD4+ T cells in the colon downmodulates Foxp3 expression (diminishing STAT5 phosphorylation) and enhances RORγt expression (by upregulating the expression of Runx1). In consequence, CD4+ T cells deprived of IL-15 rapidly trigger IBD characterized by enhanced production of pro-inflammatory cytokines (interferon-γ, IL-6) and accumulation of Th1/Th17 cells. Overall, our findings indicate a potentially beneficial role of IL-15 in IBD by fine-tuning the balance between Treg and Th17 cells and controlling intestinal inflammation.

Indexed as

Adoptive TransferAnimalsCD4-Positive T-LymphocytesCell DifferentiationColonCytokinesDown-RegulationFlow CytometryForkhead Transcription FactorsInflammatory Bowel DiseasesInterleukin-15MiceMice, KnockoutNuclear Receptor Subfamily 1, Group F, Member 3Th17 CellsTh1 CellsCytokinesForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-15Nuclear Receptor Subfamily 1, Group F, Member 3

Identifiers

PMID26964669
PMCPMC4792960
OpenAlexW2295813861

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.